A Multicenter Study of Avapritinib Efficacy and Safety of Metastatic or Unresectable Gastrointestinal Stromal Tumors

NCT05464875 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 74

Last updated 2025-02-26

No results posted yet for this study

Summary

This is a prospective, multicenter, observational real-world study to explore the therapy patterns and clinical outcomes of Avapritinib in patients with metastatic or unresectable gastrointestinal stromal tumors.

Conditions

Sponsors & Collaborators

  • Peking University Cancer Hospital & Institute

    collaborator OTHER
  • Fudan University

    collaborator OTHER
  • Peking University People's Hospital

    collaborator OTHER
  • Chinese PLA General Hospital

    collaborator OTHER
  • Xiangya Hospital of Central South University

    collaborator OTHER
  • Peking University Shenzhen Hospital

    collaborator OTHER
  • Nanfang Hospital, Southern Medical University

    collaborator OTHER
  • West China Hospital

    collaborator OTHER
  • Jiangsu Cancer Institute & Hospital

    collaborator OTHER
  • Shanghai Zhongshan Hospital

    collaborator OTHER
  • Sun Yat-sen University

    collaborator OTHER
  • Xijing Hospital

    collaborator OTHER
  • Shengjing Hospital

    collaborator OTHER
  • Shanghai Jiao Tong University School of Medicine

    collaborator OTHER
  • Liaoning Cancer Hospital & Institute

    collaborator OTHER
  • Sixth Affiliated Hospital, Sun Yat-sen University

    collaborator OTHER
  • Fujian Medical University Union Hospital

    collaborator OTHER
  • Cancer Hospital of Guangxi Medical University

    collaborator OTHER
  • Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

    collaborator OTHER
  • First Affiliated Hospital of Chongqing Medical University

    collaborator OTHER
  • Chongqing University Cancer Hospital

    collaborator OTHER
  • Xinhua Zhang, MD

    lead OTHER

Principal Investigators

  • Xinhua Zhang, PhD · First affiliated hosptial,Sun Yat-sen university

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-07-09
Primary Completion
2025-12-31
Completion
2025-12-31

Countries

  • China

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05464875 on ClinicalTrials.gov